Primary antiphospholipid syndrome
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Summary
Primary antiphospholipid syndrome (MONDO:0005204) is a disease and 5 clinical trials. Top therapeutic interventions include hydroxychloroquine. A subtype of antiphospholipid syndrome — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 5
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | primary antiphospholipid syndrome |
| Mondo ID | MONDO:0005204 |
| ICD-11 | 85700944 |
| SNOMED CT | 239892009 |
| UMLS | C0409980 |
| MedGen | 592740 |
| GARD | 0024163 |
| Is cancer (heuristic) | no |
Disease family
This is a subtype of antiphospholipid syndrome. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › syndromic disease › antiphospholipid syndrome › primary antiphospholipid syndrome
Related subtypes (3): catastrophic antiphospholipid syndrome, secondary antiphospholipid syndrome, familial antiphospholipid syndrome
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 5.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 3 |
| PHASE3 | 1 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03540810 | PHASE3 | UNKNOWN | Hydroxychloroquine Versus Placebo: Impact on Thrombotic Relapse in Primary Antiphospholipid Syndrome |
| NCT06504420 | PHASE2 | NOT_YET_RECRUITING | The Safety and Efficiency of Sirolimus in Primary Antiphospholipid Syndrome: a Randomized Control Study |
| NCT05904301 | Not specified | RECRUITING | Armenian NAtionwide REGistry of Systemic Autoimmune and Autoinflammatory Diseases |
| NCT01956188 | Not specified | UNKNOWN | Omega 3 in LES and APS |
| NCT03459508 | Not specified | COMPLETED | Ocular Findings in Women With Primary Antiphospholipid Syndrome |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| HYDROXYCHLOROQUINE | 4 | 1 |
Related Atlas pages
- Drugs: Hydroxychloroquine